A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671097



Internal ID21619402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120087501..120148992hg38UCSC Ensembl
chrX:119221459..119282898hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3861492
hg1961440
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165095
SamplesNA19238
Known GenesRHOXF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671097
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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